Reprocessed Inquiry Steerable Diagnostic EP Catheter
K-Number: K160496 · 2016-06-10
Device Summary
Frequently Asked Questions
What is the Reprocessed Inquiry Steerable Diagnostic EP Catheter?
Reprocessed Inquiry Steerable Diagnostic EP Catheter is a medical device that received FDA 510(k) clearance on 2016-06-10. It is manufactured by Innovative Health, LLC. The 510(k) number is K160496.
When was Reprocessed Inquiry Steerable Diagnostic EP Catheter approved by the FDA?
Reprocessed Inquiry Steerable Diagnostic EP Catheter received FDA 510(k) clearance on 2016-06-10, under approval number K160496.
What company makes Reprocessed Inquiry Steerable Diagnostic EP Catheter?
Reprocessed Inquiry Steerable Diagnostic EP Catheter is manufactured by Innovative Health, LLC.
What is the FDA product code for Reprocessed Inquiry Steerable Diagnostic EP Catheter?
The FDA product code for Reprocessed Inquiry Steerable Diagnostic EP Catheter is NLH.
Related Clinical Trials
Other Devices by Innovative Health, LLC
Related Devices (Code: NLH)
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.